
The most commonly reported side effects of candicidin include aspergillosis, cytomegalovirus infection, and obliterative bronchiolitis, based on 2 FDA adverse event reports from 2006 to 2024.
Percentages show how often each reaction appears relative to total reports for candicidin.
These are voluntary reports and do not establish that candicidin caused these reactions.
Report severity
Seriousness is determined by the reporter, not by OpenClaim.
Other drugs that appear in adverse event reports alongside candicidin. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
100.0% of candicidin adverse event reports involve female patients and 0.0% involve male patients. The largest age group is adult at 50%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking candicidin when the adverse event was reported.
Candicidin is sold under the brand name Vanobid.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
Ask OpenClaim about your specific drug combination. Get a sourced report using FDA data, drug labels, and medical literature.